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Hollister

EUDAMED

Class I (EU MDR)

Ref 72082

by Hollister Incorporated

Identity

Trade Name
Hollister EUDAMED
Device Name
No Touch Urethral Intermittent Catheter, Nelaton EUDAMED
Model / Reference
72082 EUDAMED

Identifiers

Primary DI / UDI-DI
00610075091928 EUDAMED
Basic UDI-DI
610075D03P092S0368DA EUDAMED
Unit of Use DI
20610075091922 EUDAMED
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use

Hollister by Hollister Incorporated — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000027818
Authorised Representative
Hollister ULC IE-AR-000022119

Sources (1)

  • EUDAMED d05f863f-d166-4087-aba8-98d0366a0327 61 fields · synced Jun 9, 2026